Reaction of diphenyldiazomethane with N-methyloxy- and N- ethyloxycarbonyl-N-(2,2,2-trichloroethylidene)amines

European Journal of Organic Chemistry

Volumn , Issue 7, 1999, Pages 1541-1544

  Jacquot, Sandrine ^a   Belaissaoui, Abdelhak ^a   Schmitt, Gérard ^a   Laude, Bernard ^a   Kubicki, Marek M ^b   Blacque, Olivier ^b  

^a UNIVERSITÉ DE FRANCHE COMTÉ   (France)

^b UNIVERSITÉ DE BOURGOGNE   (France)

Author keywords

1,3 Dipolar cycloadditions; 2 Azadiene; Aziridines; Azomethine ylides; Diphenyldiazomethane; N Alkyloxycarbonyl N (2,2,2 trichloroethylidene) amines; 3 1,3,4 Triazoline

Indexed keywords

1,3 BUTADIENE DERIVATIVE; AMINE; AZO COMPOUND; DIAZOMETHANE; FORMIC ACID DERIVATIVE; NITROGEN; TRIAZOLE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; TEMPERATURE;

EID: 0032775926     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0690(199907)1999:7<1541::AID-EJOC1541>3.0.CO;2-A     Document Type: Article

References (13)

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9. We thank the referee who suggested the alternative structure 5′a for the transient species.
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12. H. Ulrich, B. Tucker, A. A. R. Sayigh, J. Org. Chem. 1968, 33, 2887.
13. Crystallographic data for the structure 3 reported in this paper (excluding structure factors) have been deposited at the Cambridge Crystallographic Data Centre as supplementary publication number CCDC-104494. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, U.K. [Fax: (internat.) +44 (0)1223 336033; E-mail: deposit@ccdc.cam.ac.uk].